RYR2, ryanodine receptor 2, 6262

N. diseases: 160; N. variants: 116
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0035410
Disease: Rhabdomyolysis
Rhabdomyolysis
0.100 GeneticVariation phenotype GWASCAT Cerivastatin, genetic variants, and the risk of rhabdomyolysis. 21386754 2011